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Lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: Case series and literature review
INTRODUCTION: Intravenous immunoglobulin (IVIg) is currently used with considerable success for the treatment of many autoimmune diseases, including systemic lupus erythematosus (SLE). Among its various indications, IVIg has also been found to be beneficial in myocarditis, whether or not it is assoc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104142/ https://www.ncbi.nlm.nih.gov/pubmed/33950936 http://dx.doi.org/10.1097/MD.0000000000025591 |
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author | Meridor, Katya Shoenfeld, Yehuda Tayer-Shifman, Oshrat Levy, Yair |
author_facet | Meridor, Katya Shoenfeld, Yehuda Tayer-Shifman, Oshrat Levy, Yair |
author_sort | Meridor, Katya |
collection | PubMed |
description | INTRODUCTION: Intravenous immunoglobulin (IVIg) is currently used with considerable success for the treatment of many autoimmune diseases, including systemic lupus erythematosus (SLE). Among its various indications, IVIg has also been found to be beneficial in myocarditis, whether or not it is associated with an autoimmune disease. Nevertheless, data regarding IVIg treatment for myocarditis/cardiomyopathy in patients with SLE are sparse. The objective of this case series was to describe our experience with IVIg as a treatment for lupus myocarditis and to review the literature for IVIg for this indication. PATIENT CONCERNS: We report 5 female patients with SLE, who presented with signs of acute heart failure including pulmonary congestion and arrhythmias. DIAGNOSIS: Echocardiography demonstrated new reduced left ventricular ejection fraction of 20% to 30%. Two patients underwent coronary artery angiography, which demonstrated normal coronary arteries, supporting the diagnosis of myocarditis or nonischemic cardiomyopathy. INTERVENTIONS: High-dose IVIg treatment was initiated in all 5 patients. OUTCOMES: Following the treatment, clinical and echocardiographic improvement in cardiac function occurred within a few days to 1 month. This dramatic improvement persisted for several years. CONCLUSION: Based on our case series, we believe that IVIg has an important role in the management of lupus acute cardiomyopathy. This safe, well-tolerated optional treatment should be considered, especially in severe cases. |
format | Online Article Text |
id | pubmed-8104142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-81041422021-05-10 Lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: Case series and literature review Meridor, Katya Shoenfeld, Yehuda Tayer-Shifman, Oshrat Levy, Yair Medicine (Baltimore) 6900 INTRODUCTION: Intravenous immunoglobulin (IVIg) is currently used with considerable success for the treatment of many autoimmune diseases, including systemic lupus erythematosus (SLE). Among its various indications, IVIg has also been found to be beneficial in myocarditis, whether or not it is associated with an autoimmune disease. Nevertheless, data regarding IVIg treatment for myocarditis/cardiomyopathy in patients with SLE are sparse. The objective of this case series was to describe our experience with IVIg as a treatment for lupus myocarditis and to review the literature for IVIg for this indication. PATIENT CONCERNS: We report 5 female patients with SLE, who presented with signs of acute heart failure including pulmonary congestion and arrhythmias. DIAGNOSIS: Echocardiography demonstrated new reduced left ventricular ejection fraction of 20% to 30%. Two patients underwent coronary artery angiography, which demonstrated normal coronary arteries, supporting the diagnosis of myocarditis or nonischemic cardiomyopathy. INTERVENTIONS: High-dose IVIg treatment was initiated in all 5 patients. OUTCOMES: Following the treatment, clinical and echocardiographic improvement in cardiac function occurred within a few days to 1 month. This dramatic improvement persisted for several years. CONCLUSION: Based on our case series, we believe that IVIg has an important role in the management of lupus acute cardiomyopathy. This safe, well-tolerated optional treatment should be considered, especially in severe cases. Lippincott Williams & Wilkins 2021-05-07 /pmc/articles/PMC8104142/ /pubmed/33950936 http://dx.doi.org/10.1097/MD.0000000000025591 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | 6900 Meridor, Katya Shoenfeld, Yehuda Tayer-Shifman, Oshrat Levy, Yair Lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: Case series and literature review |
title | Lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: Case series and literature review |
title_full | Lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: Case series and literature review |
title_fullStr | Lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: Case series and literature review |
title_full_unstemmed | Lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: Case series and literature review |
title_short | Lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: Case series and literature review |
title_sort | lupus acute cardiomyopathy is highly responsive to intravenous immunoglobulin treatment: case series and literature review |
topic | 6900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104142/ https://www.ncbi.nlm.nih.gov/pubmed/33950936 http://dx.doi.org/10.1097/MD.0000000000025591 |
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